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5 Key Facts to Know About FDA’s Emergency Use Authorization Process

Exeed Regulatory Compliance

How Emergency Use Authorization of Medical Products Helps Provide Relief During a COVID-19 Major Crisis. The current COVID-19 global pandemic continues to remain out of control. It is a public health emergency of massive scale that has affected nearly all aspects of our life.

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How the Medical Industry Can Help Combat the Current Coronavirus Crisis

Exeed Regulatory Compliance

A novel coronavirus, now called SARS-CoV-19, was first detected in the Hubei province of China in early December 2019. Secretary of the Department of Health and Human Services (HHS) has declared a public health emergency. Global outbreak of the recent novel coronavirus needs an all-hands-on-deck approach.

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SQA Regulatory Surveillance Summary | Monthly Update 2022 – July/August

SQA

SQA Regulatory Surveillance Summary for July and August 2022. Health Canada. Counterfeit COVID-19 Antigen Rapid Test Kits Found in Ontario, 05 August 2022. Health Canada is warning consumers about counterfeit BTNX Rapid Response COVID-19 antigen rapid test kits (25-pack boxes) found in Ontario.

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The BFDs – The Ten Best Prescription Drug/Medical Device Decisions of 2023

Drug & Device Law

Executive Health Resources, Inc. , Executive Health Resources, Inc. , United States Department of Health and Human Services , 58 F.4th In 2023, these include United States ex rel. Polansky v. UnitedHealthcare, Inc. , 3d 239 (Cal. Croda Inc. , 3d 191 (Del. C-8 Personal Injury Litigation , 87 F.4th

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